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FDA FOOD RECALLS

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Every FDA food recall since 2012, in one place. We check each recall's status with FDA every day.

Checked with FDA daily · Source: U.S. Food and Drug Administration

7,366 ended recalls · showing 3,041 to 3,060

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  1. ENDEDClass II · ModerateRecalled Mar 30, 2018

    AdvoCare Nighttime Recovery Amino Acid and Herbal Dietary Supplement Product code, P3201

    Undeclared milk in a dietary supplement

    AdvoCare International, LP · Plano, TX

    Sold in the U.S. (states not listed)

    Where it was sold: United States

    Show details
    Product, as FDA describes it
    AdvoCare Nighttime Recovery Amino Acid and Herbal Dietary Supplement Product code, P3201
    Reason, in FDA's words
    Undeclared milk in a dietary supplement
    Codes on the package
    Lot numbers: 7081841, 7063321, 7052411, 7090471
    Where it was sold
    United States
    Amount recalled
    48,176 units
    Status
    Ended Sep 12, 2018 (FDA lists it as terminated)
    FDA recall number
    F-1124-2018
    View in FDA's recall database
  2. ENDEDClass II · ModerateRecalled Mar 30, 2018

    AdvoCare Muscle Strength Dietary Supplement with HMB and Suma Product code, P3221

    Undeclared milk in a dietary supplement

    AdvoCare International, LP · Plano, TX

    Sold in the U.S. (states not listed)

    Where it was sold: United States

    Show details
    Product, as FDA describes it
    AdvoCare Muscle Strength Dietary Supplement with HMB and Suma Product code, P3221
    Reason, in FDA's words
    Undeclared milk in a dietary supplement
    Codes on the package
    Lot numbers: 7063341, 7082161
    Where it was sold
    United States
    Amount recalled
    15,640 units
    Status
    Ended Sep 12, 2018 (FDA lists it as terminated)
    FDA recall number
    F-1125-2018
    View in FDA's recall database
  3. ENDEDClass III · Low riskRecalled Mar 30, 2018

    funky chunky Chocolate Pretzels. Pretzels, Caramel, Chocolate, Pecans. Sold in the following packa...

    Chocolate Pretzels are being recalled because the pecan pieces may contain undeclared tree nuts and peanuts.

    Funky Chunky LLC · Eden Prairie, MN

    Where it was sold: nationwide

    UPC 091056000458UPC 091056000403UPC 091056000847
    Show details
    Product, as FDA describes it
    funky chunky Chocolate Pretzels. Pretzels, Caramel, Chocolate, Pecans. Sold in the following packaging configurations: 1. Small Bag Net Wt. 2 oz. (56g) UPC 91056-00045; 2. Large Bag Net Wt. 5 oz. (141g) UPC 91056-00040; 3. Mini Canister Net Wt. 8 oz. (227g) UPC 91056-00084; 4. Mini Stack Gift Pack (includes 8 oz. Mini Canister Chocolate Pretzels); 5. #1506 Mixed Case, Small Bags - 25/Case (includes 5- 2 oz. bags Chocolate Pretzels) 6. Tasting Kit #1301 (includes 1-2oz. bag chocolate Pretzels) Allergen Statement: Contains: Milk, Soy, Wheat, Pecans. Manufactured in a facility that uses: Milk, Soy, Wheat, Peanuts & Tree Nuts. Funky Chunky LLC., Eden Prairie, MN 55344
    Reason, in FDA's words
    Chocolate Pretzels are being recalled because the pecan pieces may contain undeclared tree nuts and peanuts.
    Codes on the package
    Lot Code: 8B19, 8B26, 8B27, 8B28, 8C06, 8C10
    Where it was sold
    nationwide
    Amount recalled
    172 lbs.
    Status
    Ended Mar 31, 2020 (FDA lists it as terminated)
    FDA recall number
    F-1140-2018
    View in FDA's recall database
  4. ENDEDClass II · ModerateRecalled Mar 29, 2018

    Chocolate Sea Salt Probiotic Granola, Purely Elizabeth, 8oz, PET/LLDPE Pouch, 6 units/case,

    Chocolate Sea Salt Probiotic Granola due to undeclared soy lecithin.

    purely elizabeth. · Boulder, CO

    Where it was sold: Nationwide. No govt/VA/military/foreign consignees.

    Show details
    Product, as FDA describes it
    Chocolate Sea Salt Probiotic Granola, Purely Elizabeth, 8oz, PET/LLDPE Pouch, 6 units/case,
    Reason, in FDA's words
    Chocolate Sea Salt Probiotic Granola due to undeclared soy lecithin.
    Codes on the package
    Purely Elizabeth Item: 111222 Best By: OCT102017
    Where it was sold
    Nationwide. No govt/VA/military/foreign consignees.
    Amount recalled
    61 units
    Status
    Ended Aug 17, 2018 (FDA lists it as terminated)
    FDA recall number
    F-1144-2018
    View in FDA's recall database
  5. ENDEDClass II · ModerateRecalled Mar 29, 2018

    Manischewitz Brand, Dark Chocolate covered Potato Chips, 4.25 oz /12 per case, in mylar metalized ba...

    The R.A.B. Food Group LLC dba The Manischewitz Company, 80 Avenue K, Newark, NJ 07105 has initiated a recall of Manischewitz Brand, Dark Chocolate cov...

    R.A.B. Food Group LLC · Newark, NJ

    Where it was sold: Distribution states  MD, PA, WA, CT, NY, CO, CA, IL, NJ, FL, & MI, Ontatio Canada.

    Show details
    Product, as FDA describes it
    Manischewitz Brand, Dark Chocolate covered Potato Chips, 4.25 oz /12 per case, in mylar metalized bag in gable box,
    Reason, in FDA's words
    The R.A.B. Food Group LLC dba The Manischewitz Company, 80 Avenue K, Newark, NJ 07105 has initiated a recall of Manischewitz Brand, Dark Chocolate covered Potato Chips, 4.25 oz. /12 per case. because of an undeclared allergen peanut, tree nut and milk.
    Codes on the package
    Lot # 1J026
    Where it was sold
    Distribution states  MD, PA, WA, CT, NY, CO, CA, IL, NJ, FL, & MI, Ontatio Canada.
    Amount recalled
    497 Cases
    Status
    Ended Sep 1, 2021 (FDA lists it as terminated)
    FDA recall number
    F-1542-2018
    View in FDA's recall database
  6. ENDEDClass I · Most seriousRecalled Mar 28, 2018

    Ignite High Endurance Pre-Workout Supplement with Caffeine, brand Back to Health, Net wt. 1 lb. UPC...

    Ignite High Endurance Pre-Workout Supplement with Caffeine dietary supplement product is recalled because label declared WHEY protein but do not decla...

    Independent Nutrition, Inc. · Eugene, OR

    Where it was sold: CA, FL, MO, NJ, OR, TX

    UPC 801650015402UPC 801650015419
    Show details
    Product, as FDA describes it
    Ignite High Endurance Pre-Workout Supplement with Caffeine, brand Back to Health, Net wt. 1 lb. UPC 8 01650 01540 2. Ignite High Endurance Pre-Workout Supplement with CAFFEINE, brand Muscle Sports & Nutrition (MSN), Net wt. 1 lb. UPC 8 01650 01540 2 and UPC 8 01650 01541 9.
    Reason, in FDA's words
    Ignite High Endurance Pre-Workout Supplement with Caffeine dietary supplement product is recalled because label declared WHEY protein but do not declare milk.
    Codes on the package
    Back to Health brand lot #: 1502014, 1503001, 1512022, 1605004, 1105007, and 1711009. Private label brands: firm did not provide lot codes.
    Where it was sold
    CA, FL, MO, NJ, OR, TX
    Amount recalled
    Undetermined
    Status
    Ended Sep 11, 2018 (FDA lists it as terminated)
    FDA recall number
    F-1174-2018
    View in FDA's recall database
  7. ENDEDClass I · Most seriousRecalled Mar 28, 2018

    Ignite High Endurance Pre-Workout Supplement VANILLA, brand Back to Health, Net wt. 1 lb. UPC 8 016...

    Ignite High Endurance Pre-Workout Supplement VANILLA dietary supplement product is recalled because label declared WHEY protein but do not declare mi...

    Independent Nutrition, Inc. · Eugene, OR

    Where it was sold: CA, FL, MO, NJ, OR, TX

    UPC 801650015402UPC 801650015419
    Show details
    Product, as FDA describes it
    Ignite High Endurance Pre-Workout Supplement VANILLA, brand Back to Health, Net wt. 1 lb. UPC 8 01650 01540 2 and no UPC Ignite High Endurance Pre-Workout Supplement VANILLA, brand Body-B-Healthy, net wt. 1 lb. UPC 8 01650 01540 2. SAMPLE ONLY. Ignite High Endurance Pre-Workout Supplement VANILLA, brand Natures Market, net wt. 1 lb. UPC 8 01650 01541 9. SAMPLE ONLY. Ignite High Endurance Pre-Workout Supplement VANILLA, brand Alive & Well, net wt. 1 lb. UPC 8 01650 01541 9. Ignite High Endurance Pre-Workout Supplement Vanilla, brand Muscle Sports & Nutrition (MSN), net wt. 1 lb. UPC 8 01650 01540 2.
    Reason, in FDA's words
    Ignite High Endurance Pre-Workout Supplement VANILLA dietary supplement product is recalled because label declared WHEY protein but do not declare milk.
    Codes on the package
    Back to Health brand codes: 1502014, 1503001, 1512022, 1605004, 1105007, and 1711009. These two lot numbers may be found on Back to Health and Alive & Well brands: 1605007 (caffeine) and lot 1603022 (caffeine). Private label brands: firm did not provide lot codes.
    Where it was sold
    CA, FL, MO, NJ, OR, TX
    Amount recalled
    Undetermined
    Status
    Ended Sep 11, 2018 (FDA lists it as terminated)
    FDA recall number
    F-1175-2018
    View in FDA's recall database
  8. ENDEDClass I · Most seriousRecalled Mar 28, 2018

    Ignite High Endurance Pre-Workout Supplement, brand Back to Health, Net wt. 1 lb. UPC 8 01650 01541...

    Ignite High Endurance Pre-Workout Supplement dietary supplement product is recalled because label declared WHEY protein but do not declare milk.

    Independent Nutrition, Inc. · Eugene, OR

    Where it was sold: CA, FL, MO, NJ, OR, TX

    UPC 801650015419UPC 801650015402
    Show details
    Product, as FDA describes it
    Ignite High Endurance Pre-Workout Supplement, brand Back to Health, Net wt. 1 lb. UPC 8 01650 01541 9. Ignite High Endurance Pre-Workout Supplement, brand Healthy Home Center Inc., Net wt. 1 lb. UPC 8 01650 01541 9. Ignite High Endurance Pre-Workout Supplement, brand Super Natural Quality Health Food Center LLC, Net wt. 1 lb. UPC 8 01650 01540 2. SAMPLE ONLY. Ignite High Endurance Pre-Workout Supplement, brand Strike First. Net Wt. No UPC. SAMPLE ONLY.
    Reason, in FDA's words
    Ignite High Endurance Pre-Workout Supplement dietary supplement product is recalled because label declared WHEY protein but do not declare milk.
    Codes on the package
    Back to Health and Healthy Home Center brands lot #: 1502014, 1503001, 1512022, 1605004, 1105007, and 1711009. Private label brands: firm did not provide lot codes.
    Where it was sold
    CA, FL, MO, NJ, OR, TX
    Amount recalled
    Undetermined
    Status
    Ended Sep 11, 2018 (FDA lists it as terminated)
    FDA recall number
    F-1176-2018
    View in FDA's recall database
  9. ENDEDClass I · Most seriousRecalled Mar 28, 2018

    Ignite High Endurance Pre-Workout Supplement CAFFEINE FREE Formula, brand Wynant's Familty Health Fo...

    Ignite High Endurance Pre-Workout Supplement Caffeine Free dietary supplement product is recalled because label declared WHEY protein but do not decla...

    Independent Nutrition, Inc. · Eugene, OR

    Where it was sold: CA, FL, MO, NJ, OR, TX

    UPC 801650015518
    Show details
    Product, as FDA describes it
    Ignite High Endurance Pre-Workout Supplement CAFFEINE FREE Formula, brand Wynant's Familty Health Foods, Net wt. 2.64 lbs. UPC 8 01650 01551 8. SAMPLE ONLY.
    Reason, in FDA's words
    Ignite High Endurance Pre-Workout Supplement Caffeine Free dietary supplement product is recalled because label declared WHEY protein but do not declare milk.
    Codes on the package
    firm did not provide
    Where it was sold
    CA, FL, MO, NJ, OR, TX
    Amount recalled
    Undetermined
    Status
    Ended Sep 11, 2018 (FDA lists it as terminated)
    FDA recall number
    F-1177-2018
    View in FDA's recall database
  10. ENDEDClass I · Most seriousRecalled Mar 28, 2018

    Enduravol Elite Pre-Workout, brand Clean Athletics. Net wt. 1 lbs. No UPC.

    Enduravol Elite Pre-Workout dietary supplement product is recalled because label declared WHEY protein but do not declare milk.

    Independent Nutrition, Inc. · Eugene, OR

    Where it was sold: CA, FL, MO, NJ, OR, TX

    Show details
    Product, as FDA describes it
    Enduravol Elite Pre-Workout, brand Clean Athletics. Net wt. 1 lbs. No UPC.
    Reason, in FDA's words
    Enduravol Elite Pre-Workout dietary supplement product is recalled because label declared WHEY protein but do not declare milk.
    Codes on the package
    firm did not provide lot codes.
    Where it was sold
    CA, FL, MO, NJ, OR, TX
    Amount recalled
    Undetermined
    Status
    Ended Sep 11, 2018 (FDA lists it as terminated)
    FDA recall number
    F-1178-2018
    View in FDA's recall database
  11. ENDEDClass II · ModerateRecalled Mar 27, 2018

    FRANK & TONY'S NEW YORK STYLE RED ONION SAUCE, 15oz. (420g) glass jar, UPC: 6 00231 21502 2

    Product contains undeclared fish (anchovy).

    KALTEC FOOD PACKAGING INC. · Port Jervis, NY

    Where it was sold: NY

    UPC 600231215022
    Show details
    Product, as FDA describes it
    FRANK & TONY'S NEW YORK STYLE RED ONION SAUCE, 15oz. (420g) glass jar, UPC: 6 00231 21502 2
    Reason, in FDA's words
    Product contains undeclared fish (anchovy).
    Codes on the package
    Lot/Unit Numbers: 17052A
    Where it was sold
    NY
    Amount recalled
    4,704 x 15 oz. jars
    Status
    Ended Feb 8, 2019 (FDA lists it as terminated)
    FDA recall number
    F-0994-2018
    View in FDA's recall database
  12. ENDEDClass I · Most seriousRecalled Mar 27, 2018

    Wegmans Yogurt Raisins, 9 OZ (255g), in a plastic tub, UPC: 0 77890 31832 4,

    Product contains undeclared peanuts.

    First Source, LLC · Tonawanda, NY

    Where it was sold: Wegmans Stores in MA, MD, NJ, NY, PA and VA.

    UPC 077890318324
    Show details
    Product, as FDA describes it
    Wegmans Yogurt Raisins, 9 OZ (255g), in a plastic tub, UPC: 0 77890 31832 4,
    Reason, in FDA's words
    Product contains undeclared peanuts.
    Codes on the package
    BEST BEFORE 01/05/19
    Where it was sold
    Wegmans Stores in MA, MD, NJ, NY, PA and VA.
    Amount recalled
    316 cases
    Status
    Ended Apr 12, 2018 (FDA lists it as terminated)
    FDA recall number
    F-1004-2018
    View in FDA's recall database
  13. ENDEDClass II · ModerateRecalled Mar 26, 2018

    ELA ADA (JACK FRUIT), UPC: 8 70400 00085 2

    Label states ghee, but does not declare milk.

    Maharaja Food Importers, Inc. · Ridgewood, NY

    Where it was sold: Nationwide and Canada

    UPC 870400000852
    Show details
    Product, as FDA describes it
    ELA ADA (JACK FRUIT), UPC: 8 70400 00085 2
    Reason, in FDA's words
    Label states ghee, but does not declare milk.
    Codes on the package
    All lot codes, with ingredient statements that do not declare the allergen, milk, on the label.
    Where it was sold
    Nationwide and Canada
    Amount recalled
    approximatley 350-400 cases (total for all products)
    Status
    Ended Apr 5, 2019 (FDA lists it as terminated)
    FDA recall number
    F-1128-2018
    View in FDA's recall database
  14. ENDEDClass II · ModerateRecalled Mar 26, 2018

    MMRF Kumbiliappam, UPC: 87040000104, Frozen

    Label states ghee, but does not declare milk.

    Maharaja Food Importers, Inc. · Ridgewood, NY

    Where it was sold: Nationwide and Canada

    UPC 870400001040
    Show details
    Product, as FDA describes it
    MMRF Kumbiliappam, UPC: 87040000104, Frozen
    Reason, in FDA's words
    Label states ghee, but does not declare milk.
    Codes on the package
    All lot codes, with ingredient statements that do not declare the allergen, milk, on the label.
    Where it was sold
    Nationwide and Canada
    Amount recalled
    approximatley 350-400 cases (total for all products)
    Status
    Ended Apr 5, 2019 (FDA lists it as terminated)
    FDA recall number
    F-1129-2018
    View in FDA's recall database
  15. ENDEDClass II · ModerateRecalled Mar 26, 2018

    MMRF Neyyappam, UPC: 870400000111, Frozen

    Label states ghee, but does not declare milk.

    Maharaja Food Importers, Inc. · Ridgewood, NY

    Where it was sold: Nationwide and Canada

    UPC 870400000111
    Show details
    Product, as FDA describes it
    MMRF Neyyappam, UPC: 870400000111, Frozen
    Reason, in FDA's words
    Label states ghee, but does not declare milk.
    Codes on the package
    All lot codes, with ingredient statements that do not declare the allergen, milk, on the label.
    Where it was sold
    Nationwide and Canada
    Amount recalled
    approximatley 350-400 cases (total for all products)
    Status
    Ended Apr 5, 2019 (FDA lists it as terminated)
    FDA recall number
    F-1130-2018
    View in FDA's recall database
  16. ENDEDClass II · ModerateRecalled Mar 26, 2018

    Parotta Family Pack, UPC: 8 70400 00084 5, Frozen; and Small Parotta, UPC: 870400000012, Frozen

    Label states ghee, but does not declare milk.

    Maharaja Food Importers, Inc. · Ridgewood, NY

    Where it was sold: Nationwide and Canada

    UPC 870400000845UPC 870400000012
    Show details
    Product, as FDA describes it
    Parotta Family Pack, UPC: 8 70400 00084 5, Frozen; and Small Parotta, UPC: 870400000012, Frozen
    Reason, in FDA's words
    Label states ghee, but does not declare milk.
    Codes on the package
    All lot codes, with ingredient statements that do not declare the allergen, milk, on the label.
    Where it was sold
    Nationwide and Canada
    Amount recalled
    approximatley 350-400 cases (total for all products)
    Status
    Ended Apr 5, 2019 (FDA lists it as terminated)
    FDA recall number
    F-1131-2018
    View in FDA's recall database
  17. ENDEDClass II · ModerateRecalled Mar 26, 2018

    MMRF Ela Ada Jaggery, UPC: 870400000067, Frozen

    Label states ghee, but does not declare milk.

    Maharaja Food Importers, Inc. · Ridgewood, NY

    Where it was sold: Nationwide and Canada

    UPC 870400000067
    Show details
    Product, as FDA describes it
    MMRF Ela Ada Jaggery, UPC: 870400000067, Frozen
    Reason, in FDA's words
    Label states ghee, but does not declare milk.
    Codes on the package
    All lot codes, with ingredient statements that do not declare the allergen, milk, on the label.
    Where it was sold
    Nationwide and Canada
    Amount recalled
    approximatley 350-400 cases (total for all products)
    Status
    Ended Apr 5, 2019 (FDA lists it as terminated)
    FDA recall number
    F-1132-2018
    View in FDA's recall database
  18. ENDEDClass II · ModerateRecalled Mar 26, 2018

    WHOLE WHEAT PAROTTA, UPC: 8 70400 00092 0

    Label states ghee, but does not declare milk.

    Maharaja Food Importers, Inc. · Ridgewood, NY

    Where it was sold: Nationwide and Canada

    UPC 870400000920
    Show details
    Product, as FDA describes it
    WHOLE WHEAT PAROTTA, UPC: 8 70400 00092 0
    Reason, in FDA's words
    Label states ghee, but does not declare milk.
    Codes on the package
    All lot codes, with ingredient statements that do not declare the allergen, milk, on the label.
    Where it was sold
    Nationwide and Canada
    Amount recalled
    approximatley 350-400 cases (total for all products)
    Status
    Ended Apr 5, 2019 (FDA lists it as terminated)
    FDA recall number
    F-1133-2018
    View in FDA's recall database
  19. ENDEDClass II · ModerateRecalled Mar 25, 2018

    Mrs. Gerry's Kwik Trip Egg Salad, Net Wt. 35 lb. (15.87kg), UPC 17839-61135. Keep Refrigerated. Ma...

    Firm is recalling various Egg Salads and Potato Salads because they may contain undeclared traces of imitation crab meat

    Mrs Gerry's Kitchen, Inc · Albert Lea, MN

    Where it was sold: IA, IL, KS, MI, MN, MO, MT, ND, NE, SD, UT, WI

    UPC 017839611352
    Show details
    Product, as FDA describes it
    Mrs. Gerry's Kwik Trip Egg Salad, Net Wt. 35 lb. (15.87kg), UPC 17839-61135. Keep Refrigerated. Manufactured by Mrs. Gerry's, Albert Lea, MN 56007
    Reason, in FDA's words
    Firm is recalling various Egg Salads and Potato Salads because they may contain undeclared traces of imitation crab meat
    Codes on the package
    Use by: 4/13/18
    Where it was sold
    IA, IL, KS, MI, MN, MO, MT, ND, NE, SD, UT, WI
    Amount recalled
    2415 lbs.
    Status
    Ended Jun 21, 2019 (FDA lists it as terminated)
    FDA recall number
    F-1022-2018
    View in FDA's recall database
  20. ENDEDClass II · ModerateRecalled Mar 25, 2018

    Mrs. Gerry's Homestyle Egg Salad, Net Wt. 5 lb. (2.27kg), UPC 17839-60905. Keep Refrigerated. Manu...

    Firm is recalling various Egg Salads and Potato Salads because they may contain undeclared traces of imitation crab meat

    Mrs Gerry's Kitchen, Inc · Albert Lea, MN

    Where it was sold: IA, IL, KS, MI, MN, MO, MT, ND, NE, SD, UT, WI

    UPC 017839609052
    Show details
    Product, as FDA describes it
    Mrs. Gerry's Homestyle Egg Salad, Net Wt. 5 lb. (2.27kg), UPC 17839-60905. Keep Refrigerated. Manufactured by Mrs. Gerry's, Albert Lea, MN 56007
    Reason, in FDA's words
    Firm is recalling various Egg Salads and Potato Salads because they may contain undeclared traces of imitation crab meat
    Codes on the package
    Use by: 4/13/18
    Where it was sold
    IA, IL, KS, MI, MN, MO, MT, ND, NE, SD, UT, WI
    Amount recalled
    660 lbs.
    Status
    Ended Jun 21, 2019 (FDA lists it as terminated)
    FDA recall number
    F-1023-2018
    View in FDA's recall database

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What the classes mean

Class I · Most serious. FDA's highest level: products that could cause serious health problems or death.

Class II · Moderate. It may cause temporary health problems, or the risk of serious harm is remote.

Class III · Low risk. Not likely to cause health problems, but it breaks a labeling or manufacturing rule.

If you have a recalled product

  1. Match the codes on your package to the recall.
  2. If they match, don't eat it.
  3. Return it to the store or throw it away, as the company directs.
  4. If you feel sick, contact your doctor.

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Recall information comes from FDA's enforcement reports through openFDA. FDA publishes new reports weekly; we check every recall's status daily. This page is for information only and is not medical advice. Meat, poultry and egg products are recalled by USDA, not FDA, and are not listed here.